Luzzatto L - Search Results

1

Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.

Filosa S, Calabrò V, Vallone D, Poggi V, Mason P, Pagnini D, Alfinito F, Rotoli B, Martini G, Luzzatto L, et al. Filosa S, et al. Among authors: luzzatto l. Br J Haematol. 1992 Jan;80(1):111-6. doi: 10.1111/j.1365-2141.1992.tb06409.x. Br J Haematol. 1992. PMID: 1536798

2

The PNH abnormality in myeloproliferative disorders: association of PNH and acute erythremic myelosis in two children.

Luzzatto L, Familusi JB, Williams CK, Junaid TA, Rotoli B, Alfinito F. Luzzatto L, et al. Haematologica. 1979 Feb;64(1):13-30. Haematologica. 1979. PMID: 109362 No abstract available.

3

Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype.

Town M, Bautista JM, Mason PJ, Luzzatto L. Town M, et al. Among authors: luzzatto l. Hum Mol Genet. 1992 Jun;1(3):171-4. doi: 10.1093/hmg/1.3.171. Hum Mol Genet. 1992. PMID: 1303173

4

G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutation.

Ahluwalia A, Corcoran CM, Vulliamy TJ, Ishwad CS, Naidu JM, Argusti A, Stevens DJ, Mason PJ, Luzzatto L. Ahluwalia A, et al. Among authors: luzzatto l. Hum Mol Genet. 1992 Jun;1(3):209-10. doi: 10.1093/hmg/1.3.209. Hum Mol Genet. 1992. PMID: 1303182 No abstract available.

5

Purification and properties of human glucose-6-phosphate dehydrogenase made in E. coli.

Bautista JM, Mason PJ, Luzzatto L. Bautista JM, et al. Among authors: luzzatto l. Biochim Biophys Acta. 1992 Feb 13;1119(1):74-80. doi: 10.1016/0167-4838(92)90237-8. Biochim Biophys Acta. 1992. PMID: 1540638

6

Molecular heterogeneity underlying the G6PD Mediterranean phenotype.

Corcoran CM, Calabrò V, Tamagnini G, Town M, Haidar B, Vulliamy TJ, Mason PJ, Luzzatto L. Corcoran CM, et al. Among authors: luzzatto l. Hum Genet. 1992 Mar;88(6):688-90. doi: 10.1007/BF02265298. Hum Genet. 1992. PMID: 1551674

7

The molecular basis of glucose-6-phosphate dehydrogenase deficiency.

Vulliamy T, Mason P, Luzzatto L. Vulliamy T, et al. Among authors: luzzatto l. Trends Genet. 1992 Apr;8(4):138-43. doi: 10.1016/0168-9525(92)90372-B. Trends Genet. 1992. PMID: 1631957 Review.

8

[Membrane defects in paroxysmal nocturnal hemoglobinuria].

Luzzatto L, Rotoli B. Luzzatto L, et al. Haematologica. 1991 Jun;76 Suppl 3:207-12. Haematologica. 1991. PMID: 1721602 Review. Italian. No abstract available.

9

Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-.

Vulliamy TJ, Othman A, Town M, Nathwani A, Falusi AG, Mason PJ, Luzzatto L. Vulliamy TJ, et al. Among authors: luzzatto l. Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8568-71. doi: 10.1073/pnas.88.19.8568. Proc Natl Acad Sci U S A. 1991. PMID: 1924316 Free PMC article.

10

Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.

Kurdi-Haidar B, Mason PJ, Berrebi A, Ankra-Badu G, al-Ali A, Oppenheim A, Luzzatto L. Kurdi-Haidar B, et al. Among authors: luzzatto l. Am J Hum Genet. 1990 Dec;47(6):1013-9. Am J Hum Genet. 1990. PMID: 1978555 Free PMC article.

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